A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036512



Internal ID18779043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42872708..42982333hg38UCSC Ensembl
Innerchr15:43164906..43274531hg19UCSC Ensembl
Innerchr15:40952198..41061823hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38109626
hg19109626
hg18109626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552278
Samples
Known GenesTTBK2, UBR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036512
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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